A molecular defect in two families with hemolytic poikilocytic anemia: reduction of high affinity membrane binding sites for ankyrin
about
Biomechanical properties of red blood cells in health and disease towards microfluidics.Distance between Cys-201 in erythrocyte band 3 and the bilayer measured by single-photon radioluminescence.Ankyrin-G coordinates intercalated disc signaling platform to regulate cardiac excitability in vivoMolecular defect in the sickle erythrocyte skeleton. Abnormal spectrin binding to sickle inside-our vesiclesUnique alpha-spectrin mutant in a kindred with common hereditary elliptocytosis.Defective binding of spectrin to ankyrin in a kindred with recessively inherited hereditary elliptocytosisControl of erythrocyte membrane-skeletal cohesion by the spectrin-membrane linkage.Spectrin beta-chain variant associated with hereditary elliptocytosis.Molecular defect of spectrin in hereditary pyropoikilocytosis. Alterations in the trypsin-resistant domain involved in spectrin self-association.Missing band 7 membrane protein in two patients with high Na, low K erythrocytes.The spectrin membrane skeleton of normal and abnormal human erythrocytes: a review.Mutant forms of spectrin alpha-subunits in hereditary elliptocytosis.Effects of inherited membrane abnormalities on the viscoelastic properties of erythrocyte membrane.Cardiac cytoskeleton and arrhythmia: an unexpected role for protein 4.1R in cardiac excitability.
P2860
Q30402763-45710F7F-8B7B-4DF3-916B-1A7885E6F4FDQ34041065-B122E27D-8052-455B-B577-824719B99D95Q34475384-D23B68A9-EEAE-4A01-9AA3-F4E739E1BBA0Q34524564-F8DF0A94-8095-4A40-BA12-83AD452B023DQ34565862-0CC4C6C0-9062-4049-A118-55D3FF6BA954Q34613301-B229FB8C-9F8A-40D0-A7FF-5CD7349E9F6AQ34664087-60A86CA5-8E34-47EB-8106-43855CC6E5B7Q36986594-EE9059A8-F4E8-4A65-8532-6368E1F576AAQ36987699-D1456D0A-6805-4F49-891C-70EF157CA56EQ36988676-E539869B-AFD7-4C87-9FAD-38BFE8E5AAFAQ40145857-E704E0ED-5399-475A-81C1-0F7E8B5B29F0Q41014944-4A8C0996-F25C-4AB8-8778-6FF3DBE73F45Q41162109-F371C2F7-207E-40EC-BD0E-D0FBCB273EDFQ42552987-97EDC57B-C794-4EC1-A978-BCB99036C592
P2860
A molecular defect in two families with hemolytic poikilocytic anemia: reduction of high affinity membrane binding sites for ankyrin
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on December 1981
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
A molecular defect in two fami ...... rane binding sites for ankyrin
@en
A molecular defect in two fami ...... ane binding sites for ankyrin.
@nl
type
label
A molecular defect in two fami ...... rane binding sites for ankyrin
@en
A molecular defect in two fami ...... ane binding sites for ankyrin.
@nl
prefLabel
A molecular defect in two fami ...... rane binding sites for ankyrin
@en
A molecular defect in two fami ...... ane binding sites for ankyrin.
@nl
P2093
P2860
P356
P1476
A molecular defect in two fami ...... rane binding sites for ankyrin
@en
P2093
P2860
P304
P356
10.1172/JCI110411
P407
P577
1981-12-01T00:00:00Z